This is what you will do:

The individual in this position should have a working knowledge of the cGMP QC laboratory environment and  laboratory equipment associated with biopharmaceutical analysis. The QC Biochemistry Senior Analyst is responsible for providing technical and laboratory support to the QC analysts in Alexion Dublin specifically working with the team to troubleshoot issues that may arise. The position requires the ability to understand and follow written SOPs, to accurately and legibly record work in real time, and pay close attention to detail.  The individual must be able to perform routine tasks with a minimum of supervision.

You will be responsible for:

Perform all lab functions in compliance with cGMPFollow written procedures for the following tests, as trained and qualified:Gel electrophoresis (SDS-PAGE, IEF)ELISA and plate based assays (potency and residual assays such as HCP and ProA)Stability scheduling and testing.Recognize and report aberrant test results and sample conditions.Provide QC SME and day to day technical guidance to QC biochemistry analysts.Training of new analysts in specific assays.Drive continuous improvement initiatives within the QC department.Lead and complete execution of investigations/CAPAs in a timely manner.Provide lab support including reagent preparation, cleaning, and routine equipment maintenance.Ensure training is current for all job functions performed.Order, stock and receive laboratory supplies.Complete all required documentation legibly and accurately.

You will need to have:

BSc in Chemistry or a biological science, with 4-7 years’ experience, or equivalent combination of education and experience.

We would prefer for you to have:

A working knowledge of the cGMP QC laboratory environment, and equipment associated with testing of biopharmaceutical productsAbility to follow written procedures with close attention to detailAbility to function with minimal supervision for routine job duties.A working knowledge of gel electrophoresis and ELISA assays

AstraZeneca embraces diversity and equality of opportunity. We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills. We believe that the more inclusive we are, the better our work will be. We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics. We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorization and employment eligibility verification requirements.